Overview
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In this role you drive and oversee multi-site oncology trials within a global program, acting as the primary client liaison and ensuring study delivery meets scope, quality, and budget goals. You’ll lead cross-functional teams, shape trial strategy, and support business objectives through process improvement and proactive risk management. The position offers remote work across EU/UK regions and opportunities to influence senior leadership and bid defense efforts. You will partner with clients and internal teams to deliver high-impact oncology programs.
Compensaciones / Beneficios
fully remote work
work-life balance
supportive and collaborative environment
team development
opportunity to influence senior leadership
travel for bid defenses
Responsabilidades
Serve as primary client liaison and oversee client interactions, including proposals and presentations
Manage all aspects of clinical trials within assigned portfolios, ensuring consistency across studies
Provide direction to project managers across study establishment, planning, execution, procurement, and closing
Manage study budgets, identify out-of-scope work, and drive change orders
Oversee financial health: profitability, billing, and forecasting to meet business objectives
Develop or supervise robust project plans with timelines, risk management, and change management
Ensure quality management for projects, including eTMF readiness and CAPA/quality improvements




Establish and monitor trial and team progress metrics; prepare client and senior management status updates
Lead internal and client meetings; set expectations and drive study-level strategies
Oversee cross-functional teams for efficient trial execution; communicate protocol issues and corrective actions
Conduct formal presentations to diverse audiences, including bid defenses
Ensure study-specific training and compliance across functional areas
Support business development and travel for bid defenses; drive defense preparation
Mentor associate/project managers and participate in SOP updates
Provide performance feedback and address project-level issues with corrective actions
Travel domestically and internationally as required
Requisitos principales
8+ years xqbhyrx in clinical research or equivalent experience
5+ years direct project management experience
Proficient with Microsoft Office, Microsoft Project, eTMF, EDC, CTMS
Excellent communication, interpersonal, and organizational skills
Experience managing highly complex and integral studies or portfolios
Mastery of ICH-GCP and relevant SOPs; strong project management techniques
Cross-functional leadership abilities and stakeholder management
High integrity with ability to work autonomously and in teams
Proven ability to plan, negotiate, and deliver on timelines and budgets
strong communication
leadership and mentoring
cross-functional collaboration
Microsoft Office (Outlook, Word, Excel, PowerPoint)
Microsoft Project
eTMF

📌 Project Director (Barcelona)
🏢 Precision For Medicine
📍 Barcelona